Mortality after fluid bolus in African children with severe infection

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dc.contributor.author Maitland, Kathryn
dc.contributor.author Kiguli, Sarah
dc.contributor.author Opoka, Robert O.
dc.contributor.author CEngoru, Charles
dc.contributor.author Olupot-Olupot, Peter
dc.contributor.author Akech, Samuel
dc.contributor.author Nyeko, Richard
dc.contributor.author Mtove, George
dc.contributor.author Reyburn, Hugh
dc.contributor.author Lang, Trudie
dc.contributor.author Brent, Bernadette
dc.contributor.author Evans, A. Evans
dc.contributor.author Tibenderana, James K.
dc.contributor.author Crawley, Jane
dc.contributor.author Russell, Elizabeth C.
dc.contributor.author Levin, Michael
dc.contributor.author Babiker, Abdel G.
dc.contributor.author Gibb, Diana M.
dc.date.accessioned 2018-12-18T08:41:06Z
dc.date.available 2018-12-18T08:41:06Z
dc.date.issued 2011
dc.identifier.issn 1533-4406
dc.identifier.uri http://hdl.handle.net/20.500.12283/156
dc.description.abstract Background The role of fluid resuscitation in the treatment of children with shock and lifethreatening infections who live in resource-limited settings is not established. Methods We randomly assigned children with severe febrile illness and impaired perfusion to receive boluses of 20 to 40 ml of 5% albumin solution (albumin-bolus group) or 0.9% saline solution (saline-bolus group) per kilogram of body weight or no bolus (control group) at the time of admission to a hospital in Uganda, Kenya, or Tanzania (stratum A); children with severe hypotension were randomly assigned to one of the bolus groups only (stratum B). All children received appropriate antimicrobial treatment, intravenous maintenance fluids, and supportive care, according to guidelines. Children with malnutrition or gastroenteritis were excluded. The primary end point was 48-hour mortality; secondary end points included pulmonary edema, increased intracranial pressure, and mortality or neurologic sequelae at 4 weeks. Results The data and safety monitoring committee recommended halting recruitment after 3141 of the projected 3600 children in stratum A were enrolled. Malaria status (57% overall) and clinical severity were similar across groups. The 48-hour mortality was 10.6% (111 of 1050 children), 10.5% (110 of 1047 children), and 7.3% (76 of 1044 children) in the albumin-bolus, saline-bolus, and control groups, respectively (relative risk for saline bolus vs. control, 1.44; 95% confidence interval [CI], 1.09 to 1.90; P = 0.01; relative risk for albumin bolus vs. saline bolus, 1.01; 95% CI, 0.78 to 1.29; P = 0.96; and relative risk for any bolus vs. control, 1.45; 95% CI, 1.13 to 1.86; P = 0.003). The 4-week mortality was 12.2%, 12.0%, and 8.7% in the three groups, respectively (P = 0.004 for the comparison of bolus with control). Neurologic sequelae occurred in 2.2%, 1.9%, and 2.0% of the children in the respective groups (P = 0.92), and pulmonary edema or increased intracranial pressure occurred in 2.6%, 2.2%, and 1.7% (P = 0.17), respectively. In stratum B, 69% of the children (9 of 13) in the albuminbolus group and 56% (9 of 16) in the saline-bolus group died (P = 0.45). The results were consistent across centers and across subgroups according to the severity of shock and status with respect to malaria, coma, sepsis, acidosis, and severe anemia. Conclusions Fluid boluses significantly increased 48-hour mortality in critically ill children with impaired perfusion in these resource-limited settings in Africa. en_US
dc.description.sponsorship Medical Research Council, United Kingdom FEAST Current Controlled Trials en_US
dc.language.iso en en_US
dc.publisher Massachusetts Medical Society en_US
dc.subject Mortality en_US
dc.subject Fluid Bolus en_US
dc.subject African Children en_US
dc.subject Severe Infection en_US
dc.title Mortality after fluid bolus in African children with severe infection en_US
dc.type Article en_US


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